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The American Journal of Pathology logoLink to The American Journal of Pathology
. 1994 Dec;145(6):1285–1290.

Increased gelatinase A (MMP-2) and cathepsin B activity in invasive tumor regions of human colon cancer samples.

M R Emmert-Buck 1, M J Roth 1, Z Zhuang 1, E Campo 1, J Rozhin 1, B F Sloane 1, L A Liotta 1, W G Stetler-Stevenson 1
PMCID: PMC1887494  PMID: 7992833

Abstract

Gelatinase A (MMP-2) and cathepsin B are proteinases which have been proposed to participate in human tumor invasion and metastasis. Precise quantitation of the activity of these enzymes in invading tumors has not been previously described. We utilized a novel tissue microdissection technique to determine levels of enzyme activity in specific microscopic areas of invasive human colon cancer. Tissue specimens smaller than one high power field can be extracted from the samples and analyzed. Increased levels of pro-enzyme and active enzyme forms of gelatinase A (MMP-2) and increased cathepsin B activity were localized in regions of tumor invasion as compared with a matched number of normal epithelial cells from the same patient. Levels of progelatinase B (MMP-9) were also increased in the tumors; however, we did not observe activation of this enzyme. To investigate the mechanism of gelatinase A activation, we amplified DNA of specific microdissected tumor cell populations using polymerase chain reaction. We did not detect a mutation in the activation locus of the enzyme in any of the tumors studied, which suggests that activation may be due to up-regulation of a tumor-associated gelatinase A activating species. Microdissection of frozen tissue sections may prove valuable in the study of proteinases in human tumor invasion as well as in the detection of genetic alterations in human cancers.

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Selected References

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  1. Blasi F., Verde P. Urokinase-dependent cell surface proteolysis and cancer. Semin Cancer Biol. 1990 Apr;1(2):117–126. [PubMed] [Google Scholar]
  2. Campo E., Merino M. J., Liotta L., Neumann R., Stetler-Stevenson W. Distribution of the 72-kd type IV collagenase in nonneoplastic and neoplastic thyroid tissue. Hum Pathol. 1992 Dec;23(12):1395–1401. doi: 10.1016/0046-8177(92)90060-g. [DOI] [PubMed] [Google Scholar]
  3. Gong Q., Chan S. J., Bajkowski A. S., Steiner D. F., Frankfater A. Characterization of the cathepsin B gene and multiple mRNAs in human tissues: evidence for alternative splicing of cathepsin B pre-mRNA. DNA Cell Biol. 1993 May;12(4):299–309. doi: 10.1089/dna.1993.12.299. [DOI] [PubMed] [Google Scholar]
  4. Kandalaft P. L., Chang K. L., Ahn C. W., Traweek S. T., Mehta P., Battifora H. Prognostic significance of immunohistochemical analysis of cathepsin D in low-stage breast cancer. Cancer. 1993 May 1;71(9):2756–2763. doi: 10.1002/1097-0142(19930501)71:9<2756::aid-cncr2820710912>3.0.co;2-1. [DOI] [PubMed] [Google Scholar]
  5. Kane S. E., Gottesman M. M. The role of cathepsin L in malignant transformation. Semin Cancer Biol. 1990 Apr;1(2):127–136. [PubMed] [Google Scholar]
  6. Kleiner D. E., Stetler-Stevenson W. G. Quantitative zymography: detection of picogram quantities of gelatinases. Anal Biochem. 1994 May 1;218(2):325–329. doi: 10.1006/abio.1994.1186. [DOI] [PubMed] [Google Scholar]
  7. Lah T. T., Kokalj-Kunovar M., Strukelj B., Pungercar J., Barlic-Maganja D., Drobnic-Kosorok M., Kastelic L., Babnik J., Golouh R., Turk V. Stefins and lysosomal cathepsins B, L and D in human breast carcinoma. Int J Cancer. 1992 Jan 2;50(1):36–44. doi: 10.1002/ijc.2910500109. [DOI] [PubMed] [Google Scholar]
  8. Levy A. T., Cioce V., Sobel M. E., Garbisa S., Grigioni W. F., Liotta L. A., Stetler-Stevenson W. G. Increased expression of the Mr 72,000 type IV collagenase in human colonic adenocarcinoma. Cancer Res. 1991 Jan 1;51(1):439–444. [PubMed] [Google Scholar]
  9. Liotta L. A., Stetler-Stevenson W. G. Metalloproteinases and cancer invasion. Semin Cancer Biol. 1990 Apr;1(2):99–106. [PubMed] [Google Scholar]
  10. Mach L., Mort J. S., Glössl J. Noncovalent complexes between the lysosomal proteinase cathepsin B and its propeptide account for stable, extracellular, high molecular mass forms of the enzyme. J Biol Chem. 1994 Apr 29;269(17):13036–13040. [PubMed] [Google Scholar]
  11. Matrisian L. M., Bowden G. T. Stromelysin/transin and tumor progression. Semin Cancer Biol. 1990 Apr;1(2):107–115. [PubMed] [Google Scholar]
  12. Moin K., Day N. A., Sameni M., Hasnain S., Hirama T., Sloane B. F. Human tumour cathepsin B. Comparison with normal liver cathepsin B. Biochem J. 1992 Jul 15;285(Pt 2):427–434. doi: 10.1042/bj2850427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Murnane M. J., Sheahan K., Ozdemirli M., Shuja S. Stage-specific increases in cathepsin B messenger RNA content in human colorectal carcinoma. Cancer Res. 1991 Feb 15;51(4):1137–1142. [PubMed] [Google Scholar]
  14. Onisto M., Garbisa S., Caenazzo C., Freda M. P., Di Francesco C., Nitti D., Liotta L. A., Stetler-Stevenson W. G. Reverse transcription-polymerase chain reaction phenotyping of metalloproteinases and inhibitors involved in tumor matrix invasion. Diagn Mol Pathol. 1993 Jun;2(2):74–80. [PubMed] [Google Scholar]
  15. Ravdin P. M. Evaluation of cathepsin D as a prognostic factor in breast cancer. Breast Cancer Res Treat. 1993;24(3):219–226. doi: 10.1007/BF01833262. [DOI] [PubMed] [Google Scholar]
  16. Rochefort H. Biological and clinical significance of cathepsin D in breast cancer. Semin Cancer Biol. 1990 Apr;1(2):153–160. [PubMed] [Google Scholar]
  17. Rozhin J., Robinson D., Stevens M. A., Lah T. T., Honn K. V., Ryan R. E., Sloane B. F. Properties of a plasma membrane-associated cathepsin B-like cysteine proteinase in metastatic B16 melanoma variants. Cancer Res. 1987 Dec 15;47(24 Pt 1):6620–6628. [PubMed] [Google Scholar]
  18. Sheahan K., Shuja S., Murnane M. J. Cysteine protease activities and tumor development in human colorectal carcinoma. Cancer Res. 1989 Jul 15;49(14):3809–3814. [PubMed] [Google Scholar]
  19. Sinha A. A., Gleason D. F., Deleon O. F., Wilson M. J., Sloane B. F. Localization of a biotinylated cathepsin B oligonucleotide probe in human prostate including invasive cells and invasive edges by in situ hybridization. Anat Rec. 1993 Feb;235(2):233–240. doi: 10.1002/ar.1092350207. [DOI] [PubMed] [Google Scholar]
  20. Sloane B. F. Cathepsin B and cystatins: evidence for a role in cancer progression. Semin Cancer Biol. 1990 Apr;1(2):137–152. [PubMed] [Google Scholar]
  21. Sloane B. F., Rozhin J., Johnson K., Taylor H., Crissman J. D., Honn K. V. Cathepsin B: association with plasma membrane in metastatic tumors. Proc Natl Acad Sci U S A. 1986 Apr;83(8):2483–2487. doi: 10.1073/pnas.83.8.2483. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Stetler-Stevenson W. G., Aznavoorian S., Liotta L. A. Tumor cell interactions with the extracellular matrix during invasion and metastasis. Annu Rev Cell Biol. 1993;9:541–573. doi: 10.1146/annurev.cb.09.110193.002545. [DOI] [PubMed] [Google Scholar]
  23. Stetler-Stevenson W. G., Krutzsch H. C., Wacher M. P., Margulies I. M., Liotta L. A. The activation of human type IV collagenase proenzyme. Sequence identification of the major conversion product following organomercurial activation. J Biol Chem. 1989 Jan 25;264(3):1353–1356. [PubMed] [Google Scholar]
  24. Tandon A. K., Clark G. M., Chamness G. C., Chirgwin J. M., McGuire W. L. Cathepsin D and prognosis in breast cancer. N Engl J Med. 1990 Feb 1;322(5):297–302. doi: 10.1056/NEJM199002013220504. [DOI] [PubMed] [Google Scholar]

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